Venocare, Inc.
United StatesFDA applicant, unverified FDA FEI 3022728142
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Ruby Intravascular Catheter Ref K260432
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Ruby Intravascular Catheter Ref K243105
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3022728142
- DUNS number
- 118792742
- Address
- 3750 Nw 87th Ave Ste 260, Doral, FL, 33178
Frequently asked questions
How many devices does Venocare, Inc. have in the registry?
The registry currently lists 9 devices for Venocare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Venocare, Inc.'s devices?
Among its 9 most recently registered devices, Venocare, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Venocare, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Venocare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Venocare, Inc. in the registry?
The most recently registered devices listed for Venocare, Inc. include Navi Needle-free Blood Collection Device VNC20500FG, Ruby Intravascular Catheter VNC20130FG, Navi Needle-free Blood Collection Device VNC24500FG and Navi Needle-free Blood Collection Device VNC22500FG.